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International Journal of Endocrinology and Metabolism
|
January 27, 2017
A Case Series: Congenital Hyperinsulinism
Mohammad Reza Alaei, Susan Akbaroghli, Mohammad Keramatipour, et al.
Iranian Journal of Child Neurology
|
January 2, 2019
Gaucher Disease: New Expanded Classification Emphasizing Neurological Features
Mohammad Reza Alaei, Aydin Tabrizi, Narjes Jafari, et al.
Journal of Clinical and Diagnostic Research : JCDR
|
January 5, 2017
A Rare Case of Ovarian Hyperstimulation Syndrome in a Preterm Infant
Asieh Mosallanejad, Shahrzad Tabatabai, Marjan Shakiba, et al.
Iranian Biomedical Journal
|
July 26, 2016
Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient
Mohammad Reza Alaei, Saeed Talebi, Mohammad Ghofrani, et al.
Iranian Journal of Child Neurology
|
February 16, 2026
Metabolic-Immune Crosstalk in Pediatric Rheumatology: From Pathogenesis to Precision Therapy
Niloofar Shashaani, Vadood Javadi, Khosro Rahmani, et al.
Iranian Biomedical Journal
|
January 19, 2020
Once in a Blue Moon, a Very Rare Coexistence of Glutaric Acidemia Type I and Mucopolysaccharidosis Type IIIB in a Patient
Mohammad Reza Alaei, Meghdad Kheirkhahan, Saeed Talebi, et al.
Gastroenterology Research
|
March 9, 2017
Relationship Between Obesity and Liver Enzymes Levels in Turner's Syndrome
Farzaneh Rohani, Fatemeh Golgiri, Mohammad Reza Alaei, et al.
Roumanian Archives of Microbiology and Immunology
|
June 23, 2016
SEROLOGICAL RESPONSE TO VACCINES IN CHILDREN WITH DIABETES
Anahita Sanaei Dashti, Mohammad Reza Alaei, Zahra Musavi, et al.
Iranian Journal of Child Neurology
|
November 16, 2016
Chitotriosidase Activity and Gene Polymorphism in Iranian Patients with Gaucher Disease and Sibling Carriers
Hadi Mozafari, Mohammad Taghikhani, Shohreh Khatami, et al.
Journal of Clinical Laboratory Analysis
|
August 7, 2019
Mutation analysis and clinical characterization of Iranian patients with mucopolysaccharidosis type I
Mohammad Taghikhani, Shohreh Khatami, Mohammad Abdi, et al.
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Search research articles
Search
Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 3
International Journal of Endocrinology and Metabolism
|
January 27, 2017
A Case Series: Congenital Hyperinsulinism
Mohammad Reza Alaei, Susan Akbaroghli, Mohammad Keramatipour, et al.
Iranian Journal of Child Neurology
|
January 2, 2019
Gaucher Disease: New Expanded Classification Emphasizing Neurological Features
Mohammad Reza Alaei, Aydin Tabrizi, Narjes Jafari, et al.
Journal of Clinical and Diagnostic Research : JCDR
|
January 5, 2017
A Rare Case of Ovarian Hyperstimulation Syndrome in a Preterm Infant
Asieh Mosallanejad, Shahrzad Tabatabai, Marjan Shakiba, et al.
Iranian Biomedical Journal
|
July 26, 2016
Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient
Mohammad Reza Alaei, Saeed Talebi, Mohammad Ghofrani, et al.
Iranian Journal of Child Neurology
|
February 16, 2026
Metabolic-Immune Crosstalk in Pediatric Rheumatology: From Pathogenesis to Precision Therapy
Niloofar Shashaani, Vadood Javadi, Khosro Rahmani, et al.
Iranian Biomedical Journal
|
January 19, 2020
Once in a Blue Moon, a Very Rare Coexistence of Glutaric Acidemia Type I and Mucopolysaccharidosis Type IIIB in a Patient
Mohammad Reza Alaei, Meghdad Kheirkhahan, Saeed Talebi, et al.
Gastroenterology Research
|
March 9, 2017
Relationship Between Obesity and Liver Enzymes Levels in Turner's Syndrome
Farzaneh Rohani, Fatemeh Golgiri, Mohammad Reza Alaei, et al.
Roumanian Archives of Microbiology and Immunology
|
June 23, 2016
SEROLOGICAL RESPONSE TO VACCINES IN CHILDREN WITH DIABETES
Anahita Sanaei Dashti, Mohammad Reza Alaei, Zahra Musavi, et al.
Iranian Journal of Child Neurology
|
November 16, 2016
Chitotriosidase Activity and Gene Polymorphism in Iranian Patients with Gaucher Disease and Sibling Carriers
Hadi Mozafari, Mohammad Taghikhani, Shohreh Khatami, et al.
Journal of Clinical Laboratory Analysis
|
August 7, 2019
Mutation analysis and clinical characterization of Iranian patients with mucopolysaccharidosis type I
Mohammad Taghikhani, Shohreh Khatami, Mohammad Abdi, et al.
Page
of 3